SNORA101A

Summary

SNORA101A (small nucleolar RNA, H/ACA box 101A, HGNC:50405) is a gene on chromosome 4q24.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:50405
Approved symbol	SNORA101A
Name	small nucleolar RNA, H/ACA box 101A
Location	4q24
Locus type	RNA, small nucleolar
Status	Approved
Entrez	107399301
RNAcentral	URS0000A769E6 — snoRNA, 121 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 0

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

None — 0 exons

Expression profiles

Top tissues by expression

0 total, by Bgee expression score (0-100, higher = more expressed):

Regulation

Is transcription factor: no

Cross-species orthologs

0 orthologs

Protein

Protein identifiers

Canonical reviewed UniProt: None (reviewed: )

All UniProt accessions (0):

RefSeq proteins (0): (*=MANE)

Domains & families (InterPro)

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 0 (showing top):

GO Biological Process (0):

GO Molecular Function (0):

GO Cellular Component (0):

Protein interactions and networks

STRING

0 interactions, top by confidence (×1000):

IntAct

0 interactions, top by confidence:

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

0 variants total. Per-class counts are floors (≥ shown; pagination cap):

Classification	Count (floor)
Pathogenic	0
Likely pathogenic	0
Uncertain significance	0
Likely benign	0
Benign	0

Top pathogenic / likely-pathogenic (0)

SpliceAI

0 predictions. Top by Δscore:

AlphaMissense

0 scored. Top likely-pathogenic:

dbSNP variants (sampled 300 via entrez): RS1000229340 (4:100394722 A>G), RS1000620485 (4:100395944 A>G), RS1002150172 (4:100395088 A>G), RS1002536405 (4:100396333 C>T), RS1003173573 (4:100396234 G>A,T), RS1004240979 (4:100396984 A>G), RS1007514361 (4:100397134 T>C), RS1008346947 (4:100395546 T>A,C), RS1008465958 (4:100395794 A>C), RS1009290243 (4:100396279 A>G), RS1009598508 (4:100395291 T>C), RS1010949363 (4:100397104 A>G), RS1014343827 (4:100395066 A>G), RS1014741978 (4:100394738 T>A), RS1015045045 (4:100395320 C>T)

Disease associations

OMIM: gene `` | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

0 associations (top):

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 0 entries

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.